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ACTIVE NOT RECRUITING
NCT06026254
PHASE1

A Rollover Study for Subjects Who Completed Participation in IMSA101-101 Trial

Sponsor: ImmuneSensor Therapeutics Inc.

View on ClinicalTrials.gov

Summary

This is a rollover study from parent protocol IMSA101-101 for adult patients with advanced malignancies that were previously receiving IMSA101 and who would continue to receive benefit with study treatment of IMSA101 in combination with an immune checkpoint inhibitor (ICI).

Official title: Rollover Study to Continue IMSA101 Treatments in Patients With Advanced Treatment-Refractory Malignancies Previously Enrolled in the Phase I/IIA Safety and Efficacy Study of IMSA101

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

2

Start Date

2023-09-15

Completion Date

2025-09

Last Updated

2024-11-18

Healthy Volunteers

No

Interventions

DRUG

IMSA101

Intra-tumoral administration on Days 1 and 15 of every 28-day cycle

DRUG

Immune Checkpoint Inhibitor

Administered according to product label

Locations (2)

Honor Health

Scottsdale, Arizona, United States

UC San Diego Moores Cancer Center

La Jolla, California, United States